Metformin Hydrochloride
- Product NDC
- 43063-372
- 11-digit product format
- 430630372
- Labeler code
- 43063
- Product ID
- 43063-372_7d397269-7952-63f5-e053-2991aa0adee0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA076869
- Marketing category
- ANDA
- Marketing start
- 2005-04-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record